An arm support for intravenous medical treatments includes an arm support portion having a first surface and a second surface that defines a rigid support receiving zone. The first surface includes a cushioned section. At least one strap member is secured to the arm support portion. A rigid support member is positioned at the second surface at the rigid support receiving zone.

A method of reducing stress incudes measuring an initial heart rate of a user of a stress reducing system. A target heart rate for the user is selected. A musical parameter of music is played at an initial musical parameter that is associated with the initial heart rate. The musical parameter is changes until the musical parameter matches a target musical parameter that is associated with the target heart rate. A current heart rate of the user is measured. If the current heart rate does not substantially match the target heart rate, the musical parameter is changed until the musical parameter substantially matches an intermediate musical parameter, the intermediate musical parameter associated with the current heart rate. Thereafter, the musical parameter is changed until the musical parameter substantially matches the target musical parameter.

Noninvasive treatment (e.g., neuromodulation) can be achieved using vibrational energy applied via one or more wearable devices. A noninvasive treatment device includes a vibrational actuator disposed within a housing that can be secured to a user's body at or adjacent a treatment site. One or more sensors can collect physiological data before, during, or after application of vibrational energy to monitor a user's condition. Machine learning or other suitable approaches can be used to analyze sensor data to detect medical conditions and/or to effect treatment of medical conditions using devices as described herein.

The present invention relates to a skin protection device primarily comprised of a body with a top surface and a bottom surface, and a backing sheet. The body is preferably flexible and is manufactured from a biodegradable, waterproof, and UV-resistant/UV-blocking material that is plastic, fabric, or latex-based. In addition, the body may be infused with a plurality of zinc particles/compounds to protect against sun/UV damage and may have differing levels of SPF protection. The body is preferably colored to resemble the skin shade or tone of the user and has an adhesive bottom surface that can adhere to a user's skin. The body may be appropriately shaped in any conventional or non-conventional shape that may or may not mimic the shape of the body part it is being applied to.

The disclosed invention provides a skin therapy system for skin conditioning or treatment of a body part. The skin therapy system includes a body part shaped encaser including a first and second film substrate and an encaser liner disposed between the first and second film substrates. An outer peripheral edge of the encaser liner is sealed between outer peripheral edges of the first and second film substrates to create a hermetic seal forming a first fillable space between the first film substrate and a first layer of the encaser liner, a second fillable space between the second film substrate and a second layer of the encaser liner, and an internal volume defined by the first and second layers of the encaser liner and disposed between the first and second fillable spaces. The skin therapy system further includes a therapeutic composition contained within the first and second fillable spaces.

A wearable medical device comprising an annular housing configured to attach to a wrist of a patient. The wearable medical device having a first receptacle attached to the annular housing for receiving a first portion of a tube of an intravenous delivery system. The wearable medical device comprising a flow regulator attached to the annular housing and in contact with the first portion of the tube, where the flow regulator is configured to modify a geometric characteristic of the first portion of the tube. The wearable medical device further comprising a wireless transmitter for communicating with a user console.

An intravenous cuff assembly includes a cuff that is wearable around a user's arm to cover an injection site of an intravenous needle. The cuff is comprised of a resiliently stretchable material to compress against the intravenous needle thereby inhibiting movement of the intravenous needle. A plurality of first mating members and a plurality of second mating members is each coupled to the cuff. Each of the second mating members is releasably matable to a respective one of the first mating members for adjusting dimensions of the cuff. A plurality of third mating members and a plurality of fourth mating members is each coupled to the cuff. Each of the fourth mating members is releasably matable to a respective one of the third mating members for adjusting dimensions of the cuff.

A respiratory system is configured to pressurize and deliver a flow of respiratory gas to a patient's airways. The respiratory system includes a cushion configured to sealingly engage the patient's face and a blower mounted to the cushion and configured to pressurize a flow of respiratory gas. An interface structure is attached to an outlet of the blower and an aperture in the cushion. The interface structure forms a gas flow path between the cushion and the blower. The gas flow path is configured to deliver the pressurized respiratory gas from the blower through the aperture in the cushion. The gas flow path is also configured to vent exhaled gas from the aperture in the cushion to atmosphere. The respiratory system also includes headgear configured to support the cushion and the blower on the patient's face.

A negative pressure therapy dressing includes a drape layer, an adhesive border configured to provide a seal between the drape layer and skin, and a manifold layer coupled to the drape layer. The manifold layer includes a body portion extending in a first direction, a first wing positioned at a first side of the body portion, and a second wing positioned at a second side of the body portion opposite the first side. The first wing extends away from the first side and partially in the first direction such that a first gap is provided between a first tip of the first wing and the first side of the body portion. The second wing extends away from the second side and partially in the first direction such that a second gap is provided between a second tip of the second wing and the second side of the body portion.

The present invention relates to a medical treatment device for stimulating neurons of a patient. The device comprises a first non-invasive stimulating device for generating at least two different first stimuli to a patient's body, a second non-invasive stimulating device for generating at least two different second stimuli to the patient's body, and a control unit for selectively and intermittently actuating the stimulating devices. In a first operating mode, the control unit is configured to actuate the first stimulating device in a sequence of successive actuating periods such that a number n of first stimuli to be generated simultaneously during the actuating periods is variedly determined across the sequence and to actuate the second stimulating device so as to generate the second stimuli to be paired to the generation of at least a part of the first stimuli. In a second operating mode, the control unit is configured to actuate the second stimulating device so as to generate the second stimuli to be de-coupled from the generation of at least a part of the first stimuli.